Risk Adapted Therapy of Hodgkin Lymphoma in Upper Egypt

NCT ID: NCT06340243

Last Updated: 2024-04-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-04-01

Study Completion Date

2026-04-01

Brief Summary

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determine if radiotherapy could be safely omitted for early hodgkin lymphoma responder patients without compromising outcome

Detailed Description

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Hodgkin's lymphoma accounts for around 40% of all pediatric lymphomas and is the most prevalent cancer among adolescents and young adults. With combinations of chemotherapy and radiation, Hodgkin's lymphoma is roughly 80% curable, placing it among the most treatable cancers . Since the introduction of combination chemotherapy treatments 20 years ago, the prognosis for children with Hodgkin's lymphoma has improved. The treatment is mostly influenced by the stage of the disease at diagnosis, histology, existence of "B"-symptoms, and the presence of bulky disease. Nonetheless, 20% of patients do not achieve long-term remission, and around 20% experience treatment-related side effects such as secondary malignancies, infertility, cardiovascular disease, and organ malfunction following chemo-radiation .Studies of long-term therapy side effects were made possible by the significant number of survivors. The goal of therapy optimization protocols for pediatric patients with Hodgkin's lymphoma is to maintain excellent tumor control while limiting adverse effects and long-term consequences . It is critical to stratify patients based on reliable prognostic factors at presentation and according to the rapidity of response into low-risk (LR) patients who would benefit from less aggressive therapy, avoiding unnecessary toxic side effects, and high-risk (HR) patients who should be subjected to intensified therapy to reduce the rate of treatment failures and relapses .

Conditions

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Pediatric Hodgkin Lymphoma

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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radiotherapy

radiotherapy

Intervention Type RADIATION

Eligibility Criteria

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Inclusion Criteria

* Previously untreated patients younger than 18 years old with classical Hodgkin lymphoma

Exclusion Criteria

* Patients aged more than 18 years old.
* Patients who died early at presentation before starting chemotherapy
* diagnosis of nodular lymphocytic predominant Hodgkin lymphoma
* previous chemotherapy or radiotherapy other (simultaneous) malignancies
* severe concomitant diseases (eg, immune deficiency syndrome); or known HIV positive.
Minimum Eligible Age

1 Month

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Assiut University

OTHER

Sponsor Role lead

Responsible Party

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Enas Saad Hassan

principle investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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HODGKIN

Identifier Type: -

Identifier Source: org_study_id

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